酰卤
酰卤是一类含有卤素原子(如氯、溴等)和羰基官能团的化合物,通式为R-CO-X,其中R代表一个烷基、芳基或其他烃基团,X表示卤素。这类化合物因其在有机合成中具有重要应用而受到广泛关注。
1. 物理性质 酰卤通常为无色液体或固体,在常温下较为稳定,但在较高温度时会发生水解反应生成相应的羧酸和卤化氢。例如,乙酰氯(CH3COCl)是无色易挥发的油状液体,而乙酸酐(CH3CO)2O则为有刺激性气味的无色透明液体。
2. 化学性质
水解反应:酰卤能够与水迅速反应生成相应的羧酸和卤化氢气体。例如: [ R-CO-X + H_2O → R-COOH + HX ]
亲核取代反应:这类化合物也是良好的离去基团,可以用于亲核取代反应,如傅-克酰基化反应等。 [ R'-OH + R-COCl → R'-COR + HCl ]
3. 应用 酰卤因其较高的活性和选择性,在有机合成中具有重要应用价值。它们常被用来作为中间体来引入羰基,进而用于合成各种重要的药物、农药、香料等化合物。
药物合成:由于其高反应性和稳定性,酰卤常用于制备特定结构的药物分子。
合成其他化学品:通过与多种亲核试剂发生反应,可以合成酯、酸酐等多种衍生物。
总的来说,酰卤是一类多功能且广泛应用的有机化合物,在有机化学领域占据着重要位置。
中文名称 | 英文名称 | CAS号 | 化学式 | 结构式图片 |
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—— | 2-Methylidenehexanoyl fluoride | —— | C7H11FO |
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—— | Butanoyl chloride;3,3-dimethylbutanoyl chloride | —— | C10H18Cl2O2 |
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—— | cyclopentane;cyclopentanecarbonyl chloride;iron | —— | C11H9ClFeO-10 |
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—— | cyclohepta-1,4,6-trienecarbonyl chloride | —— | C8H7ClO |
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—— | (2-Hexyloxy-ethoxy)-acetyl chloride | —— | C10H19ClO3 |
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—— | 2-Cyclopenta-1,3-dien-1-ylacetyl chloride | —— | C7H7ClO |
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—— | cyclobutanecarbonyl chloride | —— | C5H7ClO |
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—— | 2,3-Dichlorobicyclo[2.1.1]hexane-5-carbonyl chloride | —— | C7H7Cl3O |
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—— | 3-cyanopropanoyl chloride | 17790-82-8 | C4H4ClNO |
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—— | allyloxyacetyl chloride | 56680-79-6 | C5H7ClO2 |
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—— | (E)-Hept-2-enoyl chloride | 76875-23-5 | C7H11ClO |
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—— | 3,5-dimethyl-1-adamantanecarbonyl chloride | 3124-87-6 | C13H19ClO |
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—— | isobutyryl iodide | 65269-91-2 | C4H7IO |
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—— | 2-cyclohexylideneacetyl chloride | 80385-43-9 | C8H11ClO |
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—— | 2-Fluoroprop-2-enoyl fluoride | 60556-85-6 | C3H2F2O |
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—— | difluoro-acetyl bromide | 814-77-7 | C2HBrF2O |
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—— | 2,2,3-trimethyl-but-3-enoyl chloride | 85620-30-0 | C7H11ClO |
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—— | 2,2-dimethylbut-3-enoyl chloride | 57690-96-7 | C6H9ClO |
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—— | 10,12-tricosadiyne-1-carbonyl chloride | 145703-55-5 | C23H37ClO |
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—— | β-Perfluorvinyl-perfluorpropionylfluorid | 36566-87-7 | C5F8O |
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—— | 2-cyclobutylacetyl chloride | 59543-38-3 | C6H9ClO |
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—— | 2,3,3,3-tetrafluoro-2-perfluorobutoxypropionyl fluoride | 65566-03-2 | C7F14O2 |
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—— | 4-Chloro-2,2,3,3,4,4-hexafluorobutanoyl fluoride | 82914-22-5 | C4ClF7O |
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—— | F(CF2)6OCF(CF3)COF | 13140-31-3 | C9F18O2 |
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—— | 2,3,3,3-tetrafluoro-2-iodopropanoyl fluoride | 83078-26-6 | C3F5IO |
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—— | perfluoro(11-cyano-2,5,8-trimethyl-3,6,9-trioxadodecanoyl) fluoride | 54716-82-4 | C13F23NO4 |
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—— | perfluoro(8-cyano-2,5-dimethyl-3,6-dioxanonanoyl) fluoride | 54716-83-5 | C10F17NO3 |
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—— | 3-Methoxytetrafluoropropionyl fluoride | 2794-15-2 | C4H3F5O2 |
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—— | 2-[2-(allyl-)hexafluorocyclobutoxy]-perfluoropropanoic acid fluoride | 155581-09-2 | C10H5F11O2 |
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—— | Perfluor-2-n-pentoxypropionylfluorid | 13140-30-2 | C8F16O2 |
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—— | 3-tert-Butyl-cyclobutanecarbonyl chloride | —— | C9H15ClO |
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—— | 2,2-difluoro-3-iodopropionyl fluoride | 99497-42-4 | C3H2F3IO |
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—— | Perfluoro-2,9-dimethyl-3,8-dioxadecandioylfluorid | 63095-44-3 | C10F18O4 |
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—— | 2-Chlor-3,3-dimethylbutanoylchlorid | 52920-18-0 | C6H10Cl2O |
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—— | Perfluoro-2-methyl-3-oxaoctandioylfluorid | 13140-22-2 | C8F14O3 |
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—— | 5-methyl-heptanoyl chloride | 107351-28-0 | C8H15ClO |
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—— | 4-Methylhexansaeurechlorid | 50599-73-0 | C7H13ClO |
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—— | 2,6-dimethyl-heptanoyl chloride | 102943-02-2 | C9H17ClO |
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—— | 2-ethyl-2-methyl-valeryl chloride | 56964-61-5 | C8H15ClO |
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—— | 4-bromopentanoic acid chloride | 221242-17-7 | C5H8BrClO |
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—— | Heptanoylfluorid | 334-19-0 | C7H13FO |
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—— | perfluoro(3-oxapentanoyl) fluoride | 13071-64-2 | C4F8O2 |
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—— | dibromofluoroacetyl fluoride | 353-98-0 | C2Br2F2O |
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—— | 3-chloropropanoyl fluoride | 7623-18-9 | C3H4ClFO |
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—— | diglycolyl difluoride | 21297-64-3 | C4F6O3 |
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—— | perfluoro-3-oxaheptanedioyl fluoride | 63095-45-4 | C6F10O3 |
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—— | Perfluoro-2-methyl-3-oxa-1,9-nonanedioyl acid difluoride | 39260-98-5 | C9F16O3 |
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—— | R-(+)-2-methoxypropionic acid chloride | 61915-18-2 | C4H7ClO2 |
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—— | (E)-5-methylhex-2-enoic acid chloride | —— | C7H11ClO |
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—— | 2-hexynoyl chloride | 7299-57-2 | C6H7ClO |
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